Results 71 to 80 of about 4,274 (211)

Regional odontodysplasia of the deciduous and permanent teeth associated with eruption disorders : a case report [PDF]

, 2008
Regional odontodysplasia (RO) is an unusual, non-hereditary anomaly of the dental hard tissues with characteristic clinical, radiographic and histological findings.
Gunhan, Omer, Gündüz, Kaan, Kurt, Murat, Zengin, Zeynep, Çelenk, Peruze, Özden, Bora   +5 more
core  

Kdf1 Regulates Molar Cusp Morphogenesis via the PI3K/AKT/mTOR Signalling Axis

Cell Proliferation, Volume 59, Issue 3, March 2026.
Epithelial Kdf1 knockout disrupts molar cusp morphogenesis by promoting inner enamel epithelium proliferation and invagination via PI3K/AKT/mTOR signalling. ABSTRACT Keratinocyte differentiation factor 1 (Kdf1) reportedly plays a significant role in enamel formation.
Jiayu Wang, Miao Yu, Hangbo Liu, Kai Sun, Chenxin Geng, Haochen Liu, Hailan Feng, Yang Liu, Hu Zhao, Dong Han   +9 more
wiley   +1 more source

ISOLATED DENTINOGENESIS IMPERFECTA AND IN ASSOCIATION WITH OSTEOGENESIS IMPERFECTA – A LITERATURE REVIEW [PDF]

Romanian Medical Journal, 2018
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic neural crest cells, continuing with their movement towards the first pharyngeal arch and leading to the development of many elements of the ...
Andrei Kozma, Doriana Agop Forna, Viorica Radoi, Ana Maria Alexandra Stanescu, Radu Ursu, Laurentiu Camil Bohaltea   +5 more
doaj   +1 more source

Reflections of Their Homelands—Early Life Enamel Formation Disruption in Nineteenth Century Settlers of Otago, New Zealand

Journal of the Royal Society of New Zealand, Volume 56, Issue 1, February 2026.
Physiological stress during early life can impede development, and signals of this are preserved in nonremodelling tissues such as dental enamel. This article describes nonspecific stress markers in the teeth of European (n = 30) and Southern Chinese (n = 15) adult migrants to New Zealand, and colony‐born children (n = 10) interred in four historic ...
Lucy A. Kavale‐Henderson, Carolina Loch, Hallie Buckley, Peter Petchey, Charlotte King, Claire Cameron, Anne Marie E. Snoddy   +6 more
wiley   +1 more source

Genetic aspects of dental disorders [PDF]

, 1998
The document attached has been archived with permission from the Australian Dental Association. An external link to the publisher’s copy is included.This paper reviews past and present applications of quantitative and molecular genetics to dental ...
Aldred MJ, Arte S., Barnett ML., Bartold PM., Baum BJ, Beaty TH, Blackwell CC, Boraas JC, Boughman JA, Boughman JA, Boughman JA, Brown T., Byers PH, Cawson RA., Cheverud JM, Chung C., Chung CS, Chung CS, Chung CS, Conneally PM, Crall MG, Crosby AH, Crowley CA, Delgado WA, Dempsey PJ, Deutsch D., DeVries RR, Elston RC., Finn SB., Fisher RA., Gedda L., George A., Goodman HO, Gorlin RJ, Hart TC., Hassell TM, Hattab FN, Houwink B., Hunt HR, Hunt HR, Hunter WS., Kaslick RS, Katz J., King L., Kirstilia V., Lagerstrom M., Laine T., Lauweryns I., Lauweryns I., Leknes KN, Lundstrom A., MacDougall M., Marazita ML, Marazita ML, Markovic MD., Michalewicz BS., Michalowicz BS, Moller E., Moss ML., Peltomaki T., Potter RH., Potter RH., Proffit WR., Reinholdt J., Roulsten D., Shapira L., Slavkin HC., Smith RJ, Takashiba S., Townsend GC, Townsend GC, Townsend GC, Townsend GC, Towsend G., Varrela J., White R., Whitney C., Willett NP, Wynne SE, Zambon JJ, Zambon JJ   +80 more
core   +1 more source

Dentin dysplasia type 1 - clinical management dilemmas: A case report of first-generation sufferers

Journal of Indian Society of Pedodontics and Preventive Dentistry, 2018
Dentine Dysplasia is a rare genetic condition. The treatment options and dilemmas associated with the condition remain undiscovered so far. This article highlights the variations in traits and challenges faced in the treatment of the cases.
Navneet Grewal, Samita Gumber, Anupam Kaur, Nirapjeet Kaur   +3 more
doaj   +1 more source

Treatment with Minicircle DNA Expressing a FGF23 Fragment in a Clinically relevant Mouse Model of X‐Linked Hypophosphatemic Rickets

Advanced Science, Volume 13, Issue 4, 19 January 2026.
The pathogenic role of PHEX isn't fully determined, and there is no radical cure for X‐linked hypophosphatemic rickets (XLHR). This study makes the first attempt to perform gene therapy using a minicircle DNA (MC‐DNA) vector expressing a fragment of FGF23 (amino acids 180‐251) in Phex‐T1349C mice and suggests MC‐DNA as a promisingly safe and effective ...
Huixiao Wu, Wanyi Zhao, Xinyu Chen, Yanzhou Wang, Shuoshuo Wei, Bo Xiang, Yingzhou Shi, Zongyue Li, Yangyang Yao, Jin Xie, Renyuan Qiu, Meng Shu, Shuo Xu, Ping Chen, Zhiying Chen, Yingjie Wu, Weibo Xia, Ling Gao, Yongfeng Song, Jiajun Zhao, Chao Xu   +20 more
wiley   +1 more source

Clinical treatment approach of a child with molar incisor hypomineralization (MIH) combined with malocclusion. [PDF]

, 2012
Introduction. Molar incisor hypomineralization (MIH) was defined as "hypomineralisation of systemic origin of permanent first molars, frequently associated with affected incisors".
Rossitza Kabaktchieva, Vladimir Bogdanov
core  

Pro-osteoclastic In Vitro Effect of Polyethylene-like Nanoparticles: Involvement in the Pathogenesis of Implant Aseptic Loosening. [PDF]

, 2016
Polyethylene micro-sized wear particles released from orthopaedic implants promote inflammation and osteolysis; however, less is known about the bioactivity of polyethylene nano-sized wear particles released from the last generation of polymer-bearing ...
Baud'huin, Benahmed, Breton, Cobelli, Cordova, Cordova, Dausend, Duplomb, Fang, Faucon, Faucon, Galvin, Glyn-Jones, Gratton, Green, Heymann, Holzapfel, Hornung, Ingram, Ma, Ma, Maitra, Matthews, Pal, Purdue, Rao, Ren, Richards, Scharf, Teletchea, Vandesompele, Yamanaka, Yamanaka, Yoshimatsu   +33 more
core   +2 more sources

Bilateral Symmetrical Fusion of Permanent Mandibular Lateral Incisors and Canines: A Rare Clinical Case

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Fusion is a rare developmental anomaly characterized by the union of two adjacent tooth germs during the morphodifferentiation stage of tooth formation, resulting in a single enlarged tooth. Its prevalence ranges from 0.4% to 0.9% in the primary dentition and approximately 0.2% in the permanent dentition.
Suresh Kandagal Veerabhadrappa, Jayanth Kumar Vadivel, Mohamed Zahoor Ul Huqh, Siddharthan Selvaraj, Anand Marya, Seema Yadav   +5 more
wiley   +1 more source